1190319-16-4
5-Bromo-3-iodo-4-azaindole
CAS: 1190319-16-4
Molecular Formula: C7H4BrIN2
1190319-16-4 - Names and Identifiers
| Name | 5-Bromo-3-iodo-4-azaindole |
| Synonyms | 5-Bromo-3-iodo-4-azaindole 5-Bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine 1H-pyrrolo[3,2-b]pyridine, 5-broMo-3-iodo- |
| CAS | 1190319-16-4 |
1190319-16-4 - Physico-chemical Properties
| Molecular Formula | C7H4BrIN2 |
| Molar Mass | 322.93 |
| Density | 2.421 |
| Storage Condition | 2-8°C |
1190319-16-4 - Introduction
5-Bromo-3-iodo-4-azaindole is an organic compound with the chemical formula BrC7H5IN2. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
5-Bromo-3-iodo-4-azaindole is a solid compound with the appearance of white crystals. It has a moderate melting and boiling point. The compound forms a solution when dissolved in an organic solvent such as ethanol and chloroform. It is a heterocyclic compound with cyclopentadiene skeleton, containing bromine, iodine and nitrogen atoms, and has certain chemical reactivity.
Use:
5-Bromo-3-iodo-4-azaindole can be used as an important intermediate in organic synthesis. It has potential applications in the field of medicine, and may be used to synthesize anti-tumor, anti-virus and anti-bacterial compounds. In addition, it can also be used in the preparation of organic light-emitting diodes as organic semiconductor materials in organic batteries and photovoltaic devices.
Preparation Method:
In general, 5-bromo-3-iodo-4-azaindole can be synthesized by an organic synthesis method. A common method is to start from indole, first carry out bromination reaction to produce 5-bromoindole, then use sodium iodide to replace bromine atom with iodine atom in iodination reaction, and finally obtain the target product by ammonia hydrogenation reaction.
Safety Information:
Because there are still few safety studies on 5-bromo-3-iodo-4-azaindole, the specific safety information is unclear. However, as an organic synthesis intermediate, it usually needs to be handled in a laboratory environment and follow relevant safety procedures, including wearing protective gloves, glasses and protective clothing, and ensuring laboratory ventilation. Care must be taken during use to avoid contact with skin and inhalation of gases. At the same time, its specific toxicity and risk need further research and evaluation before conclusion. When using or handling this compound, it is recommended to refer to the relevant information and literature and strictly follow the safety procedures.
Nature:
5-Bromo-3-iodo-4-azaindole is a solid compound with the appearance of white crystals. It has a moderate melting and boiling point. The compound forms a solution when dissolved in an organic solvent such as ethanol and chloroform. It is a heterocyclic compound with cyclopentadiene skeleton, containing bromine, iodine and nitrogen atoms, and has certain chemical reactivity.
Use:
5-Bromo-3-iodo-4-azaindole can be used as an important intermediate in organic synthesis. It has potential applications in the field of medicine, and may be used to synthesize anti-tumor, anti-virus and anti-bacterial compounds. In addition, it can also be used in the preparation of organic light-emitting diodes as organic semiconductor materials in organic batteries and photovoltaic devices.
Preparation Method:
In general, 5-bromo-3-iodo-4-azaindole can be synthesized by an organic synthesis method. A common method is to start from indole, first carry out bromination reaction to produce 5-bromoindole, then use sodium iodide to replace bromine atom with iodine atom in iodination reaction, and finally obtain the target product by ammonia hydrogenation reaction.
Safety Information:
Because there are still few safety studies on 5-bromo-3-iodo-4-azaindole, the specific safety information is unclear. However, as an organic synthesis intermediate, it usually needs to be handled in a laboratory environment and follow relevant safety procedures, including wearing protective gloves, glasses and protective clothing, and ensuring laboratory ventilation. Care must be taken during use to avoid contact with skin and inhalation of gases. At the same time, its specific toxicity and risk need further research and evaluation before conclusion. When using or handling this compound, it is recommended to refer to the relevant information and literature and strictly follow the safety procedures.
Last Update：2024-04-09 21:11:58
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